Linked Data
MyVariant Identifiers:
chr17:g.41832716G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755348G>C , CM000679.2:g.43755348G>C | GRCh38 |
| NC_000017.10:g.41832716G>C , CM000679.1:g.41832716G>C | GRCh37 |
| NC_000017.9:g.39188242G>C | NCBI36 |
| NG_008078.2:g.8441C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.636C>G MANE Select | ENSP00000301691.1:p.Ala212= | |
| ENST00000301691.2:c.636C>G | ENSP00000301691.1:p.Ala212= | |
| NM_025237.2:c.636C>G | NP_079513.1:p.Ala212= | |
| NM_025237.3:c.636C>G MANE Select | NP_079513.1:p.Ala212= |